The Global Kindness Collaborative & Global Kindness Charter

Terms of Use & Privacy Policy

Effective Date: 22 September 2026 · Last Updated: 22 September 2026

IMPORTANT NOTICE

Please read these Terms of Use and Privacy Policy carefully before using the Platform.

The Kindness Pandemic in Healthcare is a voluntary global movement intended to encourage, recognise and promote acts of kindness across healthcare organisations and communities.

The Platform is not a healthcare service, medical service, clinical service, accreditation programme, certification programme, audit, ranking or assessment of healthcare quality.

By accessing or using the Platform, registering as an individual, registering or participating on behalf of a healthcare organisation, signing the Global Kindness Charter, recording an act of kindness, sharing a practical idea or best practice, or otherwise using the Platform, you acknowledge that you have read, understood and agreed to these Terms of Use and Privacy Policy.

If you are using the Platform on behalf of a hospital, healthcare organisation, institution, company or other entity, you represent and warrant that you are authorised to do so and that you have the authority to bind that organisation to these Terms.

Part A — Terms of Use

1. About the Initiative

The Kindness Pandemic in Healthcare (“Initiative”) is a voluntary global movement intended to encourage healthcare organisations, healthcare professionals, patients, families, communities and individuals to recognise and promote acts of kindness.

The Initiative operates through the Global Kindness Collaborative, the Global Kindness Charter, and associated digital tools and resources, including this Platform.

The Platform is intended to facilitate participation in the Initiative, enable participating organisations to maintain their profiles, record or report acts of kindness, share practical ideas and best practices, and provide publicly available information regarding participating organisations and aggregate participation, where applicable.

Participation in the Initiative is entirely voluntary.

2. Definitions

For the purposes of these Terms:

  • “Platform” means the website, web application, forms, dashboards, QR-code-enabled interfaces and other digital services operated in connection with the Kindness Pandemic in Healthcare.
  • “Initiative” means The Kindness Pandemic in Healthcare and the associated Global Kindness Collaborative and Global Kindness Charter.
  • “Participating Organisation” or “Signatory Organisation” means a hospital, healthcare organisation, institution or other organisation that participates in the Initiative or signs the Global Kindness Charter.
  • “Organisation Administrator” means an individual nominated or authorised by a Participating Organisation to access or administer the organisation’s participation on the Platform.
  • “Individual User” means a person who accesses or uses the Platform in an individual capacity.
  • “Act of Kindness” means an act, interaction or instance of kindness that a user records or reports through the Platform.
  • “Personal Data” or “Personal Information” means information relating to an identified or identifiable individual, to the extent such information is regarded as personal data or personal information under applicable law.

3. Nature and Purpose of the Platform

The Platform is intended primarily to:

  1. facilitate participation in the Kindness Pandemic in Healthcare;
  2. enable healthcare organisations and individuals to record or report acts of kindness;
  3. facilitate participation in the Global Kindness Charter;
  4. enable participating hospitals and healthcare organisations to share practical ideas, experiences and best practices relating to kindness in healthcare;
  5. maintain information about participating organisations;
  6. generate aggregate participation information, statistics or counts relating to acts of kindness; and
  7. communicate with participating organisations and users regarding the Initiative.

The Platform may therefore provide participating hospitals and healthcare organisations with opportunities to share practical ideas, approaches, experiences or best practices.

Any such material must be provided only in a manner that does not disclose Personal Data, patient information, clinical information, confidential information, proprietary information or any information that could identify an individual, unless disclosure is expressly requested by the Platform and is lawful. The Platform does not require such information for the sharing of practical ideas or best practices.

The Participating Organisation is solely responsible for all information, ideas, practices, examples or other material that it submits through the Platform and for ensuring that such material complies with applicable law, confidentiality obligations and these Terms.

The Initiative does not review, verify, endorse or assume responsibility for the legality, accuracy, completeness, confidentiality or appropriateness of material submitted by a Participating Organisation.

The Platform is not intended to collect, publish or maintain personal stories, patient narratives, testimonials or identifiable accounts of individual experiences.

Users should therefore not submit stories, case descriptions, clinical narratives, patient experiences, photographs, videos, medical records or other material containing personal information through the Platform.

4. No Medical, Clinical or Healthcare Advice

The Platform does not provide medical, psychiatric, psychological, diagnostic, therapeutic, treatment or other clinical advice or services.

Nothing available through the Platform should be interpreted as medical advice, professional advice, diagnosis, treatment recommendation or clinical guidance.

Participation in the Initiative does not create a doctor-patient relationship, therapist-patient relationship, healthcare provider-patient relationship, fiduciary relationship or other professional relationship.

The Initiative does not assess, certify, verify or endorse the quality, safety, effectiveness or standard of care provided by any Participating Organisation.

Any clinical or healthcare decision remains solely the responsibility of the relevant qualified healthcare professional and healthcare organisation.

5. Voluntary Nature of the Initiative

Participation is voluntary.

The Initiative is not:

  • an accreditation body;
  • a certification programme;
  • a regulatory authority;
  • an audit programme;
  • a quality ranking system;
  • a clinical assessment;
  • a patient-safety certification;
  • a government programme; or
  • a substitute for any applicable statutory, regulatory, accreditation or professional requirement.

Recognition of participation in the Initiative does not constitute an endorsement, certification or guarantee of the quality, safety, performance or standard of care of any Participating Organisation.

Part B — Account Registration and Organisation Responsibilities

6. Eligibility and Accurate Information

Users and Participating Organisations must provide information that is accurate, current, complete and not misleading.

A Participating Organisation is solely responsible for the accuracy, completeness, legality and currency of information that it provides to the Platform.

The Initiative is entitled to rely on information supplied by a Participating Organisation and is not required to independently verify every item of information supplied by that organisation.

The Initiative shall not be responsible for any loss, claim, dispute, representation, misrepresentation or consequence arising from inaccurate, incomplete, misleading, outdated or unauthorised information supplied by a Participating Organisation or its representatives.

7. Hospital and Healthcare Organisation Authorisation

Where an individual registers, signs the Charter, creates or manages a profile, shares information or best practices, records an Act of Kindness, or otherwise acts on behalf of a hospital or healthcare organisation, that individual represents and warrants that they are duly authorised to act on behalf of that organisation.

The Participating Organisation is solely responsible for:

  1. determining who is authorised to represent it;
  2. ensuring that only authorised personnel access its organisation profile;
  3. ensuring that the email addresses used for organisational access belong to authorised personnel;
  4. ensuring that access is removed or transferred when an authorised individual changes role, leaves the organisation, resigns, retires or otherwise ceases to be authorised;
  5. maintaining the security and confidentiality of organisational login credentials;
  6. monitoring activity undertaken through its organisational account; and
  7. promptly notifying the Initiative of any suspected or actual unauthorised access or misuse.

The Initiative shall not be responsible for any access or activity resulting from the failure of a Participating Organisation to properly manage its authorised personnel, credentials or access rights.

8. Responsibility When Personnel Leave an Organisation

A Participating Organisation must promptly deactivate, revoke or otherwise terminate the access of any person who:

  • leaves the organisation;
  • resigns;
  • retires;
  • changes employment or role;
  • ceases to be an authorised representative; or
  • is otherwise no longer authorised to access the Platform on behalf of the organisation.

The Participating Organisation acknowledges that the Initiative cannot reasonably determine, on a continuous basis, whether an individual remains employed or authorised by an organisation.

Accordingly, the organisation bears primary responsibility for managing its authorised users and access credentials.

9. Account and Password Security

Where the Platform requires a password, authentication credential, verification code or other account credential, the user is responsible for maintaining its confidentiality and security.

Users must:

  • keep passwords and authentication credentials confidential;
  • not share credentials with unauthorised persons;
  • use reasonable security precautions;
  • immediately notify the Initiative if they suspect that their account or credentials have been compromised; and
  • log out or otherwise secure access where appropriate.

All activity carried out through an organisation’s account may be attributed to that organisation unless and until the Initiative receives appropriate notice of suspected unauthorised access.

The Initiative shall not be liable for losses arising from a user’s failure to maintain appropriate account or credential security, except to the extent liability cannot lawfully be excluded.

Part C — Acts of Kindness, Ideas, Best Practices and Prohibited Information

10. Recording Acts of Kindness

The Platform may enable users to record or report an Act of Kindness.

The purpose of this functionality is to record participation and, where applicable, generate aggregate counts or statistics.

The Platform is not intended to collect personal stories or identifiable narratives.

Users should submit only the minimum information necessary to record an Act of Kindness.

11. Sharing Practical Ideas and Best Practices

Participating hospitals and healthcare organisations may be provided with an opportunity to share practical ideas, approaches, experiences, learnings or best practices relating to kindness in healthcare.

Such contributions are intended for knowledge sharing and peer learning.

Any organisation submitting such material is solely responsible for ensuring that the material:

  • does not contain Personal Data or Personal Information relating to any individual;
  • does not identify or enable the identification of a patient, family member, employee, healthcare professional or other individual;
  • does not contain medical records, clinical information or health information relating to an identifiable person;
  • does not contain confidential or privileged information;
  • does not disclose proprietary or commercially sensitive information without appropriate authority;
  • does not breach any applicable law, contractual obligation, professional duty or confidentiality obligation; and
  • does not infringe the rights of any third party.

The Initiative does not require Participating Organisations to disclose Personal Data or confidential information in order to share a practical idea or best practice.

If an organisation nevertheless submits such information, the entire responsibility and liability arising from that submission shall rest with the submitting organisation, subject to applicable law. The Initiative shall not be responsible for the organisation’s failure to comply with its own privacy, confidentiality, employment, contractual, professional or legal obligations.

The Initiative may remove, redact, anonymise, restrict or decline to publish any such material where it becomes aware that the material may contain Personal Data, confidential information or other prohibited content.

12. Strict Prohibition on Personal or Confidential Information

Users expressly agree not to submit, upload, disclose, publish or otherwise enter through the Platform any Personal Data or Personal Information relating to themselves or any other person unless expressly requested and legally permitted by the Platform.

This prohibition applies to all areas and functionalities of the Platform, including organisation profiles, practical ideas, best practices, Acts of Kindness, forms, comments, submissions, communications and any other fields or features.

In particular, users must not submit:

  • names of patients, family members or healthcare professionals in connection with a specific act;
  • telephone numbers;
  • email addresses;
  • residential addresses;
  • photographs or videos identifying individuals;
  • medical records;
  • hospital records;
  • clinical notes;
  • diagnoses;
  • treatment information;
  • prescriptions;
  • laboratory or imaging reports;
  • medical identification numbers;
  • government identification numbers;
  • insurance information;
  • passwords or authentication credentials;
  • information relating to a person’s health or mental health;
  • information about minors;
  • confidential employment information;
  • confidential hospital or institutional information; or
  • any other information that could identify or reasonably be used to identify an individual.

Users must also not use the Platform to disclose confidential, privileged, proprietary or commercially sensitive information belonging to a hospital, healthcare organisation, employer, patient or third party.

Users expressly undertake that they will not use the Platform as a means of sharing personal, patient, clinical or confidential information.

If a user inadvertently submits such information, the user must promptly notify the Initiative at dralok_k@apollohospitals.com.

The Initiative may remove, restrict, anonymise or otherwise deal with such information where reasonably necessary.

13. Responsibility for Information Submitted

Each user is solely responsible for the information they submit through the Platform.

A Participating Organisation is solely responsible for information submitted or entered by persons acting on its behalf.

By submitting information, the user represents and warrants that:

  1. the information is accurate to the best of their knowledge;
  2. the submission does not violate applicable law;
  3. the submission does not infringe another person’s rights;
  4. the submission does not contain prohibited Personal Data or confidential information;
  5. the user has the necessary authority to submit the information; and
  6. the submission does not expose the Initiative or any third party to an unlawful claim or liability.

14. Right to Remove or Restrict Information

The Initiative reserves the right, without prior notice, to remove, disable, restrict, modify or decline to display any information, account, profile or participation record where it reasonably believes that:

  • these Terms have been breached;
  • applicable law may have been violated;
  • the information is inaccurate, misleading or unauthorised;
  • the information contains Personal Data or confidential information;
  • the account may have been compromised;
  • the information may create legal, regulatory, security or reputational risk; or
  • such action is otherwise reasonably necessary to protect the Platform, users, Participating Organisations or the Initiative.

The Initiative is not required to provide prior notice before taking such action where immediate action is reasonably necessary.

Part D — Privacy Policy

15. Information We Collect

Depending on how the Platform is used, we may collect the following categories of information.

15.1 Individual Users

For individual participation, we may collect:

  • name, where provided;
  • email address;
  • mobile number, where voluntarily provided;
  • authentication or account information;
  • participation information;
  • records of Acts of Kindness or participation counts; and
  • technical information necessary to operate, secure and maintain the Platform.

15.2 Participating Organisations

For participating hospitals and healthcare organisations, we may collect:

  • organisation name;
  • organisation location;
  • official organisation details;
  • name of authorised representative;
  • designation;
  • official email address;
  • mobile or telephone number, where provided;
  • details of Organisation Administrators;
  • verification information and/or supporting documents provided for organisational verification; and
  • information relating to the organisation’s participation in the Initiative.

15.3 Verification Information

Where verification is required, the Platform may request documents or information reasonably necessary to establish that an organisation or representative is authorised to participate.

Such information is used for verification and administrative purposes and is not intended for public display unless expressly stated otherwise.

16. What We Do Not Intend to Collect

The Initiative does not intentionally seek to collect:

  • patient medical records;
  • clinical information;
  • diagnoses;
  • treatment information;
  • health histories;
  • patient narratives;
  • personal testimonials;
  • identifiable kindness stories;
  • photographs or videos of individuals; or
  • other unnecessary Personal Data.

Users must not voluntarily provide such information through the Platform.

17. How We Use Information

Information collected through the Platform may be used to:

  1. create and administer user or organisation accounts;
  2. verify participating organisations and authorised representatives;
  3. maintain participation records;
  4. display participating organisation information where applicable;
  5. record aggregate participation and Acts of Kindness;
  6. generate aggregate statistics and reports;
  7. communicate with users and Participating Organisations regarding the Initiative;
  8. maintain, secure, troubleshoot and improve the Platform;
  9. prevent fraud, misuse, unauthorised access or other security incidents;
  10. comply with applicable legal, regulatory or governmental requirements; and
  11. protect the rights, safety and legitimate interests of the Initiative, users and Participating Organisations.

We will not sell Personal Data as a commercial product.

18. Publicly Displayed Information

The Platform may publicly display limited information relating to Participating Organisations, such as:

  • organisation name;
  • city, state, country or general location;
  • participation status;
  • Charter participation;
  • aggregate participation information; and
  • aggregate counts or other non-identifying information relating to Acts of Kindness.

Individual users’ email addresses, mobile numbers and other private account information will not be publicly displayed merely because an individual participates in the Initiative.

The Initiative may publish aggregate or anonymised information for awareness, research, reporting, educational or promotional purposes, provided that such information is not intended to identify an individual.

19. Legal Basis and Applicable Data-Protection Laws

The Initiative seeks to process Personal Data in accordance with applicable data-protection and privacy laws.

Depending on the jurisdiction and circumstances, processing may be based on consent, contractual necessity, legitimate or lawful purposes, compliance with legal obligations, or another lawful basis recognised under applicable law.

Where applicable law provides individuals with rights concerning their Personal Data, the Initiative will provide mechanisms for exercising those rights subject to applicable legal requirements and limitations.

Because the Initiative is intended to operate internationally, privacy rights may differ depending upon the user’s country or jurisdiction.

20. Data Minimisation

The Initiative follows a data-minimisation approach and seeks to collect only information reasonably necessary for the operation, administration, security and legitimate purposes of the Platform.

Users should not provide information that is not requested or necessary.

In particular, users should never use an Act of Kindness entry, practical idea, best-practice submission or any other Platform feature to disclose information about another individual.

21. Data Sharing and Disclosure

The Initiative does not sell Personal Data.

Personal Data may be disclosed or made accessible where reasonably necessary:

  • to operate and maintain the Platform;
  • to service providers or technology providers acting on behalf of the Initiative;
  • for verification and administration;
  • for security and fraud prevention;
  • to comply with applicable law or a lawful governmental request;
  • to establish, exercise or defend legal rights; or
  • where otherwise permitted or required by applicable law.

Where third-party service providers process Personal Data on behalf of the Initiative, the Initiative may require appropriate contractual, organisational or technical safeguards, as applicable.

22. International Use and Cross-Border Processing

The Initiative is intended to operate globally.

Accordingly, information may be processed, stored or accessed in countries other than the country in which a user or Participating Organisation is located, subject to applicable law.

By using the Platform, users acknowledge that international participation may involve cross-border processing or access.

The Initiative will take such measures as may be required under applicable law in relation to international transfers of Personal Data.

23. Data Security

The Initiative seeks to implement reasonable technical and organisational safeguards designed to protect information against unauthorised access, alteration, disclosure, loss or misuse.

However, no website, database, electronic transmission or internet-based service can be guaranteed to be completely secure.

Accordingly, the Initiative does not warrant that the Platform will be completely secure, uninterrupted, error-free or immune from cyberattacks, hacking, malware, data breaches or other security incidents.

Users and Participating Organisations are responsible for taking reasonable precautions on their own devices, networks and accounts.

24. Security Incidents

If the Initiative becomes aware of a security incident affecting Personal Data, it will take reasonable steps required under applicable law, which may include investigating the incident, taking containment and remediation measures and making legally required notifications.

Nothing in these Terms makes the Initiative an insurer against security incidents or transfers to the Initiative responsibility for security failures occurring solely because of a user’s or Participating Organisation’s own systems, devices, credentials, personnel or security practices.

25. Data Retention

Personal Data will be retained only for as long as reasonably necessary for the purposes for which it was collected, for legitimate operational purposes, for compliance with applicable legal obligations, or for the establishment, exercise or defence of legal claims.

When Personal Data is no longer reasonably required, it may be deleted, anonymised or otherwise securely disposed of, subject to applicable law and legitimate retention requirements.

Aggregate or anonymised participation information may be retained for longer periods because such information is not intended to identify individual users.

26. Individual Privacy Rights

Subject to applicable law, individuals may have rights relating to their Personal Data, including rights to:

  • request access to Personal Data;
  • request correction of inaccurate Personal Data;
  • request deletion or erasure where legally applicable;
  • withdraw consent where processing is based on consent;
  • request information regarding processing; and
  • lodge a complaint or seek other available remedies under applicable law.

Requests may be submitted to dralok_k@apollohospitals.com.

The Initiative may need to verify the identity and authority of the person making a request before taking action.

Part E — Organisation-Specific Responsibilities

27. Responsibility of Participating Organisations

Each Participating Organisation acknowledges that it is responsible for:

  • the accuracy of its information;
  • the identity and authority of its representatives;
  • the security of its organisational accounts;
  • management of Organisation Administrators;
  • removal of access when personnel leave or cease to be authorised;
  • ensuring that its personnel comply with these Terms;
  • ensuring that it does not upload or submit patient or other Personal Data;
  • ensuring that it complies with applicable privacy, confidentiality and healthcare laws;
  • ensuring that it has all necessary internal permissions and authorisations for participation;
  • ensuring that any practical ideas, experiences or best practices submitted through the Platform do not contain Personal Data, patient information or confidential information; and
  • any activity undertaken by persons using its account or acting in its name.

The Initiative does not assume responsibility for the internal employment, access-control, privacy, confidentiality or information-security practices of a Participating Organisation.

28. Unauthorised Use of a Hospital’s Name

If a Participating Organisation becomes aware that:

  • an unauthorised person is using its name;
  • an unauthorised person has created or accessed an account on its behalf;
  • its publicly displayed profile is inaccurate or fraudulent; or
  • an individual is falsely representing themselves as an authorised representative,

the organisation should immediately notify dralok_k@apollohospitals.com.

The Initiative may, upon receiving appropriate information, suspend the relevant access, temporarily disable the profile, remove or correct the publicly displayed information, or take other reasonable action pending verification.

The Initiative does not assume responsibility for independently monitoring employment status or organisational authority on an ongoing basis.

Part F — Acceptable Use

29. Prohibited Conduct

Users must not:

  1. use the Platform for unlawful purposes;
  2. impersonate another person or organisation;
  3. falsely claim authority to represent a hospital or healthcare organisation;
  4. submit false or misleading information;
  5. submit Personal Data relating to themselves or another person where it is not specifically requested and legally permitted;
  6. submit patient, clinical or medical information;
  7. upload malicious code, malware, viruses or other harmful material;
  8. attempt to gain unauthorised access to another user’s account or the Platform;
  9. interfere with the security or operation of the Platform;
  10. scrape, harvest or systematically collect Personal Data from the Platform without permission;
  11. use the Platform to send spam or unsolicited commercial communications;
  12. infringe intellectual property, privacy, confidentiality or other rights of another person or organisation;
  13. use the Platform to make defamatory, discriminatory, threatening or unlawful statements;
  14. misuse QR codes, verification mechanisms or organisational accounts; or
  15. circumvent any security, access-control or verification mechanism.

30. Suspension and Termination

The Initiative may suspend, restrict or terminate access to the Platform where reasonably necessary, including where:

  • these Terms are breached;
  • an account is suspected to be compromised;
  • unauthorised access is suspected;
  • false or misleading information has been provided;
  • unlawful or prohibited information is submitted;
  • continued access creates security, legal or regulatory risk; or
  • the Platform or Initiative is discontinued.

A Participating Organisation may voluntarily withdraw from the Initiative at any time by contacting the Initiative.

Termination or withdrawal does not affect provisions that by their nature are intended to survive termination, including provisions concerning confidentiality, intellectual property, liability, indemnity, dispute resolution and applicable law.

Part G — Intellectual Property

31. Ownership of the Platform

Unless otherwise stated, the Platform, its software, design, branding, graphics, logos, text, databases, functionality and other materials are owned by or licensed to the Initiative or its relevant licensors.

Users receive only a limited, non-exclusive, non-transferable and revocable right to use the Platform for its intended purposes.

No ownership rights are transferred to users through use of the Platform.

32. Organisation Names and Logos

Participating Organisations may permit the Initiative to display their organisation name, logo or other identifying information for the limited purpose of identifying participation in the Initiative, subject to applicable permissions and these Terms.

A Participating Organisation may request correction or removal of its publicly displayed information by contacting dralok_k@apollohospitals.com.

The Initiative may remove or modify such information where reasonably necessary.

33. Aggregate and Anonymised Information

The Initiative may use aggregated, statistical or anonymised information relating to participation and Acts of Kindness for purposes including:

  • awareness;
  • educational activities;
  • research;
  • reporting;
  • presentations;
  • publications;
  • programme evaluation;
  • communications;
  • advocacy for kindness in healthcare; and
  • promotion of the Initiative.

Such use will not intentionally identify individual users where the information has been anonymised or aggregated.

Part H — Disclaimers

34. Platform Provided “As Is”

To the maximum extent permitted by applicable law, the Platform and its contents are provided on an “as is” and “as available” basis.

The Initiative does not warrant that:

  • the Platform will always be available;
  • the Platform will be uninterrupted;
  • the Platform will be error-free;
  • information will always be complete or accurate;
  • the Platform will be compatible with every device or system;
  • the Platform will be free from viruses or other harmful components; or
  • the Platform will be completely secure.

35. No Endorsement of Organisations

Listing, recognition or participation of a hospital or healthcare organisation on the Platform does not constitute:

  • accreditation;
  • certification;
  • regulatory approval;
  • quality certification;
  • patient-safety certification;
  • clinical endorsement;
  • endorsement of medical professionals;
  • endorsement of treatment outcomes; or
  • a guarantee of the organisation’s performance.

Participation reflects participation in a voluntary movement and nothing more.

36. Third-Party Websites and Services

The Platform may contain links to third-party websites, services, applications or resources.

The Initiative does not control and is not responsible for the content, security, privacy practices, availability or policies of third-party services.

Users access third-party services at their own risk and should review the relevant third party’s terms and privacy policies.

Part I — Limitation of Liability

37. Limitation of Liability

To the fullest extent permitted by applicable law, the Initiative, the Global Kindness Collaborative, their respective partners, affiliates, officers, directors, employees, consultants, volunteers, agents, technology providers and service providers shall not be liable for any indirect, incidental, special, consequential, exemplary or punitive loss or damage arising out of or relating to:

  • use of or inability to use the Platform;
  • participation in the Initiative;
  • information supplied by a user or Participating Organisation;
  • practical ideas, experiences, best practices or other material submitted by a Participating Organisation;
  • unauthorised access to an account;
  • misuse of organisational credentials;
  • acts or omissions of a Participating Organisation or Organisation Administrator;
  • information displayed on the Platform;
  • reliance on information available through the Platform;
  • technical interruptions or failures;
  • cyberattacks or security incidents;
  • third-party services;
  • loss of data;
  • loss of business, reputation, opportunity or goodwill; or
  • any other matter arising from participation in or use of the Initiative.

To the fullest extent permitted by applicable law, the Initiative shall not be responsible for matters that are within the control or responsibility of a user or Participating Organisation, including the security of their own devices, networks, credentials, personnel and internal systems, or their failure to comply with applicable privacy and confidentiality obligations.

Nothing in these Terms excludes or limits liability that cannot lawfully be excluded or limited under applicable law.

Part J — Indemnity

38. Indemnification by Users and Organisations

To the fullest extent permitted by applicable law, each user and each Participating Organisation agrees to indemnify, defend and hold harmless the Initiative, the Global Kindness Collaborative, their partners, officers, directors, employees, consultants, volunteers, agents and service providers from and against claims, demands, proceedings, losses, liabilities, damages, penalties, costs and expenses, including reasonable legal expenses, arising out of or relating to:

  1. the user’s or organisation’s breach of these Terms;
  2. false, inaccurate or misleading information supplied by the user or organisation;
  3. unauthorised use of an organisation’s account;
  4. failure to properly manage organisational access;
  5. acts or omissions of an Organisation Administrator;
  6. submission or disclosure of Personal Data or confidential information;
  7. submission of patient, clinical or health information;
  8. submission of practical ideas, experiences, best practices or other material that infringes privacy, confidentiality, intellectual property or other rights;
  9. violation of privacy, confidentiality, intellectual property or other rights of a third party;
  10. unlawful use of the Platform;
  11. misuse of the Platform or its verification mechanisms; or
  12. any claim arising from information or material submitted by or on behalf of the user or organisation.

This indemnity is intended to apply to matters arising from the user’s or Participating Organisation’s own acts, omissions, representations or breaches and does not extend to liability that cannot lawfully be shifted under applicable law.

Part K — Governing Law and Disputes

39. Governing Law

These Terms shall be governed by and interpreted in accordance with the laws of India, except to the extent that mandatory provisions of the law applicable to a particular user cannot legally be excluded.

Subject to applicable mandatory rights and laws, courts having jurisdiction at New Delhi, India shall have jurisdiction over disputes arising from or relating to these Terms or the Platform.

Nothing in this clause is intended to deprive a user of mandatory consumer, privacy or other statutory rights available in the user’s jurisdiction.

Part L — Changes and General Provisions

40. Changes to these Terms

The Initiative may modify, update or replace these Terms from time to time.

The updated version will be published on the Platform with a revised “Last Updated” or “Effective Date”.

Continued use of the Platform after the updated Terms become effective constitutes acceptance of the revised Terms, to the extent permitted by applicable law.

Where applicable law requires specific notice or consent for material changes, the Initiative will take the measures required by that law.

41. Severability

If any provision of these Terms is determined to be invalid, unlawful or unenforceable, that provision shall be interpreted or modified to the minimum extent necessary to make it enforceable, where legally possible.

The remaining provisions shall continue in full force and effect.

42. No Waiver

Failure by the Initiative to enforce any provision of these Terms shall not constitute a waiver of its right to enforce that provision in the future.

43. Entire Agreement

These Terms, together with any other policies or notices expressly incorporated by reference, constitute the agreement governing use of the Platform in relation to the matters covered by these Terms.

They supersede earlier versions of the Platform’s Terms of Use and Privacy Policy relating to the same subject matter, except to the extent that a separate written agreement expressly provides otherwise.

44. No Agency or Partnership

Participation in the Initiative does not create any partnership, joint venture, employment, agency, franchise, fiduciary or other legal relationship between the Initiative and any Participating Organisation or Individual User.

A Participating Organisation may not represent that it is an agent of, or has authority to bind, the Initiative unless expressly authorised in writing.

45. Force Majeure

The Initiative shall not be responsible for delay, interruption or failure to perform caused by circumstances beyond its reasonable control, including natural disasters, war, terrorism, civil unrest, government action, epidemics, telecommunications failures, internet outages, infrastructure failures, cyber incidents, labour disruptions or failures of third-party service providers.

Part M — Contact

46. Contact Us

For questions regarding these Terms, privacy, account access, organisational verification, suspected unauthorised access, removal or correction of organisation information, or privacy-related requests, please contact:

Dr. Alok K
Email: dralok_k@apollohospitals.com

You may also contact:
Dr. Naveen G
Email: drnaveen_g@apollohospitals.com

For suspected unauthorised use of a hospital or healthcare organisation’s name, account or profile, the concerned organisation should notify the Initiative as soon as reasonably possible so that appropriate verification, suspension, correction or removal action can be considered.

47. Acknowledgement

By using the Platform, the user acknowledges that:

  • participation in the Kindness Pandemic in Healthcare is voluntary;
  • the Platform is not a medical or clinical service;
  • the user will not submit Personal Data or confidential information relating to themselves or any other person unless expressly requested and legally permitted;
  • the user will not include Personal Data or confidential information in practical ideas, experiences or best-practice submissions;
  • the user is responsible for the security of their own account and credentials;
  • a Participating Organisation is responsible for its authorised users and account access;
  • a Participating Organisation must promptly remove access when a representative ceases to be authorised;
  • information supplied by a user or organisation is their responsibility;
  • any practical ideas, experiences, best practices or other material submitted by a Participating Organisation are the responsibility of that organisation;
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Effective Date: 22 September 2026 · Last Updated: 22 September 2026